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Health Canada Medical devices

ViziShot 2 Flex

Issued February 4, 2026
Issue
Olympus is removing all unexpired ViziShot 2 Flex (19g) devices due to a potential patient safety issue. Customers should not use any of the affected devices listed in the medical device recall letter and should return any affected products. Olympus is also reinforcing existing warnings in the Instructions for Use (IFU).
Hazard description
Labelling and packaging - Performance
Product
Product name
ViziShot 2 Flex
Reference
ID
RA-77960